US9309254B2 - Pyrimidinyl-diazospiro compounds - Google Patents

Pyrimidinyl-diazospiro compounds Download PDF

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US9309254B2
US9309254B2 US14/403,480 US201314403480A US9309254B2 US 9309254 B2 US9309254 B2 US 9309254B2 US 201314403480 A US201314403480 A US 201314403480A US 9309254 B2 US9309254 B2 US 9309254B2
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methyl
phenyl
pyrimidin
diazaspiro
nonan
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US20150119404A1 (en
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Gerard M. P. Giblin
David T. MacPherson
David R. Witty
Steven J. Stanway
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Convergence Pharmaceuticals Ltd
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Convergence Pharmaceuticals Ltd
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    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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Definitions

  • the invention relates to spiro derivatives, to the use of said derivatives in treating diseases and conditions mediated by modulation of voltage-gated sodium channels, to compositions containing said derivatives and processes for their preparation.
  • Voltage-gated sodium channels are responsible for the initial phase of the action potential, which is a wave of electrical depolarisation usually initiated at the soma of the neuron and propagated along the axon to the terminals. At the terminals, the action potential triggers the influx of calcium and the release of neurotransmitter.
  • Drugs such as lidocaine
  • Other sodium channel blockers such as lamotrigine and carbamazepine are used to treat epilepsy. In the latter case, partial inhibition of voltage-gated sodium channels reduces neuronal excitability and reduces seizure propagation.
  • the voltage-gated sodium channel family is made up of 9 subtypes, four of which are found in the brain, NaV1.1, 1.2, 1.3 and 1.6. Of the other subtypes, NaV1.4 is found only in skeletal muscle, NaV1.5 is specific to cardiac muscle, and NaV1.7, 1.8, and 1.9 are found predominantly in sensory neurons.
  • the hypothesised binding site for state-dependent sodium channel blockers is the local anaesthetic (LA) binding site in the inner vestibule of the pore on transmembrane S6 of domain IV.
  • LA local anaesthetic
  • Critical residues are located in a highly conserved region among the different subtypes, thus presenting a challenge for the design of new subtype selective drugs. Drugs such as lidocaine, lamotrigine and carbamazepine do not distinguish between the subtypes. However, selectivity can be achieved, and can be further enhanced functionally, as a result of the different frequencies at which the channels operate.
  • Drugs that block voltage-gated sodium channels in a state-dependent manner are also used in the treatment of bipolar disorder, either to reduce symptoms of mania or depression, or as mood stabilisers to prevent the emergence of mood episodes.
  • Clinical and preclinical evidence also suggests that state-dependent sodium channel blockers may help to reduce the symptoms of schizophrenia.
  • lamotrigine has been shown to reduce symptoms of psychosis induced by ketamine in healthy human volunteers, and furthermore, studies in patients suggest that the drug can augment the antipsychotic efficacy of some atypical antipsychotic drugs, such as clozapine or olanzapine. It is hypothesised that efficacy in these psychiatric disorders may result in part from a reduction of excessive glutamate release. The reduction in glutamate release is thought to be a consequence of sodium channel inhibition in key brain areas, such as the frontal cortex. However, interaction with voltage-gated calcium channels may also contribute to the efficacy of these drugs.
  • WO 2007/042240 (Glaxo Group Limited) describes a series of quaternary alpha-aminocarboxamide derivatives as modulators of voltage-gated sodium channels.
  • the object of the invention is to identify alternative compounds which modulate voltage-gated sodium channels.
  • the invention provides a compound of formula (I) or a pharmaceutically acceptable salt or solvate thereof:
  • Ring A represents a phenyl ring, a 5- or 6-membered aromatic heterocyclic ring or a 5- to 12-membered aromatic or non-aromatic bicyclic heterocyclic group
  • n represents an integer selected from 0 to 4
  • each R 1 independently represents C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, -Z—C 3-6 cycloalkyl, halogen, haloC 1-6 alkyl, C 1-6 alkoxy, haloC 1-6 alkoxy, -Z-phenyl, -Z-Het, —CN, —CONR 6 R 7 , —NR 6 R 7 , -Z—C 1-3 alkyl, wherein said Het group represents a 5- or 6-membered aromatic heterocyclic ring or a 4- to 7-membered non-aromatic heterocyclic ring, wherein said phenyl or Het group of R 1 may be optionally substituted by one or more (e.
  • Ring A represents a phenyl ring, a 5- or 6-membered aromatic heterocyclic ring or a 5- to 12-membered aromatic or non-aromatic bicyclic heterocyclic group
  • n represents an integer selected from 0 to 4
  • each R 1 independently represents C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, -Z—C 3-6 cycloalkyl, halogen, haloC 1-6 alkyl, C 1-6 alkoxy, haloC 1-6 alkoxy, -Z-phenyl, -Z-Het, —CN, —CONR 6 R 7 , —NR 6 R 7 , -Z—C 1-3 alkyl, wherein said Het group represents a 5- or 6-membered aromatic heterocyclic ring or a 4- to 7-membered non-aromatic heterocyclic ring, wherein said phenyl or Het group of R 1 may be optionally substituted by one or more (e.
  • R 8 groups and wherein n represents an integer greater than 1, said R 1 groups represent no more than one -Z-phenyl or one -Z-Het group; Z represents a bond or a linker selected from —O—, —CH 2 —, —CH 2 —O— or O—CH 2 —; R 6 and R 7 independently represent hydrogen or C 1-6 alkyl or R 6 and R 7 together with the nitrogen atom to which they are attached join to form a 4- to 7-membered nitrogen containing non-aromatic heterocyclic ring; R 8 represents C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, halogen, haloC 1-6 alkyl, C 1-6 alkoxy, haloC 1-6 alkoxy, —CN or —NR 6 R 7 ; m represents an integer selected from 0 to 2; each R 2 independently represents C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl,
  • halo or ‘halogen’ as used herein refers to fluorine, chlorine, bromine or iodine.
  • C 1-3 alkyl refers to a linear or branched saturated hydrocarbon group containing from 1 to 3 carbon atoms.
  • C 1-6 alkyl refers to a linear or branched saturated hydrocarbon group containing from 1 to 6 carbon atoms. Examples of such groups include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, neopentyl or hexyl and the like.
  • C 2-6 alkenyl as used herein as a group or part of a group refers to a linear or branched hydrocarbon group containing from 2 to 6 carbon atoms and containing a carbon carbon double bond.
  • C 2-6 alkynyl as used herein as a group or part of a group refers to a linear or branched hydrocarbon group having from 2 to 6 carbon atoms and containing a carbon carbon triple bond.
  • C 1-6 alkoxy as used herein as a group or part of a group refers to an —O—C 1-6 alkyl group wherein C 1-6 alkyl is as defined herein. Examples of such groups include methoxy, ethoxy, propoxy, butoxy, and the like.
  • haloC 1-6 alkyl refers to a C 1-6 alkyl group as defined herein wherein one or more than one hydrogen atom is replaced with a halogen.
  • the term ‘haloC 1-6 alkyl’ therefore includes monohaloC 1-6 alkyl and also polyhaloC 1-6 alkyl. There may be one, two, three or more hydrogen atoms replaced with a halogen, so the haloC 1-6 alkyl may have one, two, three or more halogens. Examples of such groups include fluoroethyl, fluoromethyl, trifluoromethyl or trifluoroethyl and the like.
  • haloC 1-6 alkoxy refers to a O—C 1-6 alkyl group as defined herein wherein one or more than one hydrogen atom is replaced with a halogen.
  • the term ‘haloC 1-6 alkoxy’ therefore includes monohaloC 1-6 alkoxy, and also polyhaloC 1-6 alkoxy. There may be one, two, three or more hydrogen atoms replaced with a halogen, so the haloC 1-6 alkoxy may have one, two, three or more halogens. Examples of such groups include fluoroethyloxy, difluoromethoxy or trifluoromethoxy and the like.
  • 5- or 6-membered aromatic heterocyclic ring means a heterocyclyl group containing one or more carbon atoms, one or more hydrogen atoms and one or more heteroatoms such as nitrogen, oxygen and sulfur; the carbon and heteroatoms being interconnected to form a ring.
  • five membered aromatic heterocyclic groups include but are not limited to pyrrole, furan, thiophene, imidazole, furazan, oxazole, oxadiazole, oxatriazole, isoxazole, thiazole, thiadiazole, isothiazole, pyrazole, triazole and tetrazole groups.
  • six membered aromatic heterocyclic groups include but are not limited to pyridine, pyrazine, pyridazine, pyrimidine and triazine.
  • non-aromatic heterocyclic ring means a heterocyclyl group containing one or more carbon atoms, one or more hydrogen atoms and one or more heteroatoms such as nitrogen, oxygen and sulfur; the carbon and heteroatoms being interconnected to form a ring.
  • non-aromatic embraces, unless the context indicates otherwise, unsaturated ring systems without aromatic character, partially saturated and fully saturated heterocyclyl ring systems.
  • unsaturated and “partially saturated” refer to rings wherein the ring structure(s) contains atoms sharing more than one valence bond i.e. the ring contains at least one multiple bond e.g. a C ⁇ C, C ⁇ C or N ⁇ C bond.
  • saturated or “fully saturated” refers to rings where there are no multiple bonds between ring atoms.
  • Particular examples include morpholine, piperidine (e.g. 1-piperidinyl, 2-piperidinyl, 3-piperidinyl and 4-piperidinyl), piperidone, pyrrolidine (e.g.
  • preferred non-aromatic heterocyclyl groups include saturated groups such as piperidine, pyrrolidine, azetidine, morpholine, piperazine and N-alkyl piperazines.
  • nitrogen containing non-aromatic heterocyclic ring means a non-aromatic heterocyclyl ring as defined herein wherein the ring must contain at least one ring nitrogen atom.
  • nitrogen-containing non-aromatic heterocyclyl groups include aziridine, morpholine, thiomorpholine, piperidine (e.g. 1-piperidinyl, 2-piperidinyl, 3-piperidinyl and 4-piperidinyl), pyrrolidine (e.g.
  • Particular examples of 5- to 12-membered bicyclic heterocyclic groups typically comprise groups containing a five membered ring fused to another five membered ring and include but are not limited to imidazothiazole (e.g. imidazo[2,1-b]thiazole) and imidazoimidazole (e.g. imidazo[1,2-a]imidazole).
  • imidazothiazole e.g. imidazo[2,1-b]thiazole
  • imidazoimidazole e.g. imidazo[1,2-a]imidazole
  • 5- to 12-membered bicyclic heterocyclic groups typically comprise groups containing a six membered ring fused to a five membered ring and include but are not limited to benzofuran, benzothiophene, benzimidazole, benzoxazole, isobenzoxazole, benzisoxazole, benzthiazole, benzisothiazole, isobenzofuran, indole, isoindole, indolizine, indoline, isoindoline, purine (e.g., adenine, guanine), indazole, pyrazolopyrimidine (e.g.
  • pyrazolo[1,5-a]pyrimidine triazolopyrimidine (e.g. [1,2,4]triazolo[1,5-a]pyrimidine), benzodioxole, imidazopyridine and pyrazolopyridine (e.g. pyrazolo[1,5-a]pyridine) groups.
  • 5- to 12-membered bicyclic heterocyclic groups typically comprise groups containing two fused six membered rings and include but are not limited to quinoline, isoquinoline, chroman, thiochroman, isochroman, chromene, isochromene, benzodioxan, quinolizine, benzoxazine, pyridopyridine, quinoxaline, quinazoline, cinnoline, phthalazine, naphthyridine and pteridine groups.
  • 5- to 12-membered bicyclic heterocyclic groups typically comprise groups containing an aromatic ring and a non-aromatic ring and include, tetrahydroisoquinoline, tetrahydroquinoline, dihydrobenzthiophene, dihydrobenzfuran, 2,3-dihydro-benzo[1,4]dioxine, benzo[1,3]dioxole, 4,5,6,7-tetrahydrobenzofuran, tetrahydrotriazolopyrazine (e.g.
  • substituted means substituted by one or more defined groups.
  • groups may be selected from a number of alternative groups, the selected groups may be the same or different.
  • Ring A represents a phenyl ring, a 5- or 6-membered aromatic heterocyclic ring (such as thiophenyl) or a 5- to 12-membered aromatic or non-aromatic bicyclic heterocyclic group (such as indolyl or benzodioxolyl). In a further embodiment, Ring A represents a phenyl ring.
  • n represents an integer selected from 0 to 3. In a further embodiment, n represents an integer selected from 1 to 2. In one embodiment, n represents 1. In an alternative embodiment, n represents 2.
  • R 1 independently represents C 1-6 alkyl (such as methyl, ethyl or isopropyl), halogen (such as fluorine or chlorine), haloC 1-6 alkyl (such as CF 3 ), C 1-6 alkoxy (such as —O-methyl, —O-ethyl, —O-propyl, —O-butyl, —O—CH(Me) 2 or —O—CH 2 —CH(Me) 2 ), haloC 1-6 alkoxy (such as —O—CF 3 , —OCHF 2 or —CH 2 —O—CF 3 ), -Z-aryl (such as —O-phenyl, —O—CH 2 -phenyl or —CH 2 —O-phenyl), —CN, —CONR 6 R 7 (such as CONH 2 ) or —NR 6 R 7 (such as —N(Me) 2 ), wherein said phenyl groups are
  • R 1 independently represents C 1-6 alkyl (such as methyl), halogen (such as fluorine or chlorine), haloC 1-6 alkyl (such as CF 3 ), C 1-6 alkoxy (such as —O-methyl, —O-ethyl or —O—CH(Me) 2 ), haloC 1-6 alkoxy (such as —O—CF 3 or —OCHF 2 ), —CN or —CONR 6 R 7 (such as CONH 2 ).
  • C 1-6 alkyl such as methyl
  • halogen such as fluorine or chlorine
  • haloC 1-6 alkyl such as CF 3
  • C 1-6 alkoxy such as —O-methyl, —O-ethyl or —O—CH(Me) 2
  • haloC 1-6 alkoxy such as —O—CF 3 or —OCHF 2
  • —CN or —CONR 6 R 7 such as CONH 2
  • R 1 independently represents halogen (such as fluorine or chlorine), haloC 1-6 alkyl (such as CF 3 ), C 1-6 alkoxy (such as —O-methyl, —O-ethyl or —O—CH(Me) 2 ) or haloC 1-6 alkoxy (such as —O—CF 3 or —OCHF 2 ).
  • halogen such as fluorine or chlorine
  • haloC 1-6 alkyl such as CF 3
  • C 1-6 alkoxy such as —O-methyl, —O-ethyl or —O—CH(Me) 2
  • haloC 1-6 alkoxy such as —O—CF 3 or —OCHF 2
  • R 1 independently represents halogen (such as fluorine), haloC 1-6 alkyl (such as CF 3 ), C 1-6 alkoxy (such as —O-ethyl) or haloC 1-6 alkoxy (such as —O—CF 3 ).
  • halogen such as fluorine
  • haloC 1-6 alkyl such as CF 3
  • C 1-6 alkoxy such as —O-ethyl
  • haloC 1-6 alkoxy such as —O—CF 3
  • R 1 independently represents haloC 1-6 alkyl (such as CF 3 ).
  • Z represents —O—, —CH 2 —O— or —O—CH 2 —.
  • R 6 and R 7 independently represent hydrogen or C 1-6 alkyl. In a further embodiment, R 6 and R 7 independently represent hydrogen or methyl. In yet a further embodiment, R 6 and R 7 both represent hydrogen.
  • R 8 represents halogen (e.g. fluorine or chlorine) or haloC 1-6 alkoxy (e.g. —O—CF 3 ).
  • m represents an integer selected from 0 to 1. In one embodiment, m represents 1. In an alternative embodiment, m represents 0.
  • R 2 independently represents C 1-6 alkyl, halogen, haloC 1-6 alkyl, C 1-6 alkoxy or haloC 1-6 alkoxy. In a further embodiment, R 2 independently represents C 1-6 alkyl (such as methyl), halogen (such as fluorine) or C 1-6 alkoxy (such as —OC(Me) 3 ). In a further embodiment, R 2 independently represents C 1-6 alkyl (such as methyl).
  • R 3 represents hydrogen or methyl. In a further embodiment, R 3 represents hydrogen.
  • R 4 represents hydrogen, methyl or ethyl. In a further embodiment, R 4 represents hydrogen or methyl.
  • R 5 independently represents C 1-3 alkyl (such as methyl) or fluoro. In a further embodiment, R 5 represents methyl or fluoro. In a yet further embodiment, R 5 represents methyl. In an alternative embodiment, R 5 represents fluoro. In one embodiment, p represents 0 to 2. In a further embodiment, p represents 0. In an alternative embodiment, p represents 2. For the avoidance of doubt it should be stated that R 5 may be present at any position on either of the spiro rings.
  • Y represents a —CH 2 — group. In an alternative embodiment, Y represents a —(CH 2 ) 2 — group.
  • q represents 0 or 1. In a further embodiment, q represents 0. In an alternative embodiment, q represents 2.
  • R 9 represents methyl
  • the invention provides a compound of formula (I) a or a pharmaceutically acceptable salt or solvate thereof:
  • R 4a represents hydrogen or methyl.
  • the compound of formula (I) a is a compound selected from Example 7 and Examples 39 to 42.
  • the compound of formula (I) a is a compound selected from Example 7, the free base of Example 7 and Examples 7a and 7b.
  • the invention provides a compound of formula (I) b or a pharmaceutically acceptable salt or solvate thereof:
  • R 4a represents hydrogen or methyl.
  • the compound of formula (I) b is a compound selected from Example 7 and Example 39. In a further embodiment, the compound of formula (I) b is a compound selected from Example 7, the free base of Example 7 and Examples 7a and 7b.
  • the compound of formula (I) is:
  • the compound of formula (I) is a compound of E1-E22 or an alternative pharmaceutically acceptable salt, solvate or free base preparation thereof.
  • the compound of formula (I) is (2R,5S)-7-methyl-2-[4-methyl-6-[4-(trifluoromethyl)-phenyl]pyrimidin-2-yl]-1,7-diazaspiro[4.4]nonan-6-one or a pharmaceutically acceptable salt or solvate thereof, such as (2R,5S)-7-methyl-2-[4-methyl-6-[4-(trifluoromethyl)-phenyl]pyrimidin-2-yl]-1,7-diazaspiro[4.4]nonan-6-one hydrochloride (E7).
  • the compound of formula (I) is (2R,5S)-7-methyl-2-[4-methyl-6-[4-(trifluoromethyl)-phenyl]pyrimidin-2-yl]-1,7-diazaspiro[4.4]nonan-6-one mono sulfuric acid salt (E7a) or (2R,5S)-7-methyl-2-[4-methyl-6-[4-(trifluoromethyl)-phenyl]pyrimidin-2-yl]-1,7-diazaspiro[4.4]nonan-6-one monosulfuric acid salt hydrate (E7b).
  • the compound of formula (I) is the free base of E7, i.e. (2R,5S)-7-methyl-2-[4-methyl-6-[4-(trifluoromethyl)-phenyl]pyrimidin-2-yl]-1,7-diazaspiro[4.4]nonan-6-one.
  • the compound of formula (I) is other than 7-methyl-2-[4-methyl-6-[4-(trifluoromethyl)-phenyl]pyrimidin-2-yl]-1,7-diazaspiro[4.4]nonan-6-one or a pharmaceutically acceptable salt or solvate thereof, such as:
  • the compound of formula (I) is a compound of E1-E6 and E8-E46. In a further embodiment, the compound of formula (I) is a compound of E1-E6 or E8-E22.
  • a reference to a compound of the formula (I) and sub-groups thereof also includes ionic forms, salts, solvates, isomers (including geometric and stereochemical isomers), tautomers, N-oxides, esters, prodrugs, isotopes and protected forms thereof, for example, as discussed below; preferably, the salts or tautomers or isomers or N-oxides or solvates thereof; and more preferably, the salts or tautomers or N-oxides or solvates thereof, even more preferably the salts or tautomers or solvates thereof.
  • the salts of the present invention can be synthesized from the parent compound that contains a basic or acidic moiety by conventional chemical methods such as methods described in Pharmaceutical Salts: Properties, Selection, and Use , P. Heinrich Stahl (Editor), Camille G. Wermuth (Editor), ISBN: 3-90639-026-8, Hardcover, 388 pages, August 2002.
  • such salts can be prepared by reacting the free acid or base forms of these compounds with the appropriate base or acid in water or in an organic solvent, or in a mixture of the two; generally, nonaqueous media such as dichloromethane, 1,4-dioxane, ether, ethyl acetate, ethanol, isopropanol, or acetonitrile are used.
  • Acid addition salts may be formed with a wide variety of acids, both inorganic and organic.
  • acid addition salts include mono- or di-salts formed with an acid selected from the group consisting of acetic, 2,2-dichloroacetic, adipic, alginic, ascorbic (e.g.
  • D-glucuronic D-glucuronic
  • glutamic e.g. L-glutamic
  • ⁇ -oxoglutaric glycolic, hippuric
  • hydrohalic acids e.g. hydrobromic, hydrochloric, hydriodic
  • isethionic lactic (e.g.
  • salts consist of salts formed from acetic, hydrochloric, hydriodic, phosphoric, nitric, sulfuric, citric, lactic, succinic, maleic, malic, isethionic, fumaric, benzenesulfonic, toluenesulfonic, sulfuric, methanesulfonic (mesylate), ethanesulfonic, naphthalenesulfonic, valeric, acetic, propanoic, butanoic, malonic, glucuronic and lactobionic acids.
  • One particular salt is the hydrochloride salt.
  • Another particular salt is the hydrogensulfate.
  • the compounds of the invention may exist as mono- or di-salts depending upon the pKa of the acid from which the salt is formed.
  • the salt forms of the compounds of the invention are typically pharmaceutically acceptable salts, and examples of pharmaceutically acceptable salts are discussed in Berge et al., 1977, “Pharmaceutically Acceptable Salts,” J. Pharm. Sci ., Vol. 66, pp. 1-19. However, salts that are not pharmaceutically acceptable may also be prepared as intermediate forms which may then be converted into pharmaceutically acceptable salts. Such non-pharmaceutically acceptable salts forms, which may be useful, for example, in the purification or separation of the compounds of the invention, also form part of the invention.
  • solvates complexes with solvents in which they are reacted or from which they are precipitated or crystallized. These complexes are known as “solvates”.
  • solvates a complex with water is known as a “hydrate”.
  • Pharmaceutically acceptable solvates of the compound of the invention are within the scope of the invention.
  • the pharmaceutically acceptable solvates of the compounds of the invention include the hydrate thereof.
  • N-oxides are the N-oxides of a tertiary amine or a nitrogen atom of a nitrogen-containing heterocycle.
  • N-Oxides can be formed by treatment of the corresponding amine with an oxidizing agent such as hydrogen peroxide or a per-acid (e.g. a peroxycarboxylic acid), see for example Advanced Organic Chemistry , by Jerry March, 4th Edition, Wiley Interscience, pages. More particularly, N-oxides can be made by the procedure of L. W. Deady ( Syn. Comm. 1977, 7, 509-514) in which the amine compound is reacted with m-chloroperoxybenzoic acid (MCPBA), for example, in an inert solvent such as dichloromethane.
  • MCPBA m-chloroperoxybenzoic acid
  • the invention provides compounds of formula (Ia)
  • R 1 , R 2 , R 3 , R 4 , R 5 , R 9 , m, n, p, q, Y and A are as defined herein for compounds of formula (I).
  • q represents 0.
  • the invention provides compounds of formula (Ib)
  • R 1 , R 2 , R 3 , R 4 , R 5 , R 9 , m, n, p, q, A and Y are as defined herein for compounds of formula (I).
  • q represents 0.
  • the invention provides compounds of formula (Ic)
  • R 1 , R 2 , R 3 , R 4 , R 5 , R 9 , m, n, p, q, A and Y are as defined herein for compounds of formula (I).
  • q represents 0.
  • the invention provides compounds of formula (Id)
  • R 1 , R 2 , R 3 , R 4 , R 5 , R 9 , m, n, p, q, A and Y are as defined herein for compounds of formula (I).
  • q represents 0.
  • the present invention includes all pharmaceutically acceptable isotopically-labeled compounds of the invention, i.e. compounds of formula (I), wherein one or more atoms are replaced by atoms having the same atomic number, but an atomic mass or mass number different from the atomic mass or mass number usually found in nature.
  • isotopes suitable for inclusion in the compounds of the invention comprise isotopes of hydrogen, such as 2 H (D) and 3 H (T), carbon, such as 11 C, 13 C and 14 C, chlorine, such as 36 Cl, fluorine, such as 18 F, iodine, such as 123 I, 125 I and 131 I, nitrogen, such as 13 N and 15 N, oxygen, such as 15 O, 17 O and 18 O, phosphorus, such as 32 P, and sulfur, such as 35 S.
  • hydrogen such as 2 H (D) and 3 H (T)
  • carbon such as 11 C, 13 C and 14 C
  • chlorine such as 36 Cl
  • fluorine such as 18 F
  • iodine such as 123 I, 125 I and 131 I
  • nitrogen such as 13 N and 15 N
  • oxygen such as 15 O, 17 O and 18 O
  • phosphorus such as 32 P
  • sulfur such as 35 S.
  • Certain isotopically-labelled compounds of formula (I), for example, those incorporating a radioactive isotope, are useful in drug and/or substrate tissue distribution studies.
  • the compounds of formula (I) can also have valuable diagnostic properties in that they can be used for detecting or identifying the formation of a complex between a labelled compound and other molecules, peptides, proteins, enzymes or receptors.
  • the detecting or identifying methods can use compounds that are labelled with labelling agents such as radioisotopes, enzymes, fluorescent substances, luminous substances (for example, luminol, luminol derivatives, luciferin, aequorin and luciferase), etc.
  • the radioactive isotopes tritium, i.e. 3 H (T), and carbon-14, i.e. 14 C, are particularly useful for this purpose in view of their ease of incorporation and ready means of detection.
  • Substitution with heavier isotopes such as deuterium, i.e. 2 H (D), may afford certain therapeutic advantages resulting from greater metabolic stability, for example, increased in vivo half-life or reduced dosage requirements, and hence may be preferred in some circumstances.
  • Isotopically-labeled compounds of formula (I) can generally be prepared by conventional techniques known to those skilled in the art or by processes analogous to those described in the accompanying Examples and Preparations using an appropriate isotopically-labeled reagents in place of the non-labeled reagent previously employed.
  • Process (a) typically comprises treating the compound of formula (II) with a suitable reagent, such as silver trifluoromethanesulfonate (AgOTf), with stirring at a suitable temperature, such as 40° C., for a suitable time period, such as 3 to 7 days, followed by reduction of the resulting imine (IIA) by a hydride reducing agent such as sodium triacetoxyborohydride in a solvent system such as aqueous hydrochloride acid and dichloromethane, or by using borane or a modified borane such as tertiarybutylamine:borane complex, or hydrogenation over a suitable catalyst such as platinum.
  • a suitable reagent such as silver trifluoromethanesulfonate (AgOTf)
  • a suitable time period such as 3 to 7 days
  • L 1 represents a suitable leaving group, such as a halogen atom (i.e. bromine) and L 2 represents a suitable leaving group, such as a halogen atom (i.e. iodine) and P 1 represents a suitable protecting group, such as Boc.
  • Step (i) typically comprises reacting a compound of formula (III) with a compound of formula (IV) in the presence of a suitable solvent, such as dichloroethane (DCE).
  • a suitable solvent such as dichloroethane (DCE).
  • Step (ii) typically comprises reacting a compound of formula (V) with a compound of formula (VI) in the presence of a suitable base such as potassium tert-butoxide and a suitable solvent, such as tetrahydrofuran (THF).
  • a suitable base such as potassium tert-butoxide
  • a suitable solvent such as tetrahydrofuran (THF).
  • Step (iii) typically comprises deprotecting a compound of formula (VII) with a suitable acidic reagent, such as citric acid.
  • Step (iv) comprises a chiral resolution in which one chiral diastereomeric salt form of (VIII) is crystallised and separated from a more soluble epimer, for example by fractional crystallisation of (VIII) with a chiral acid such as mandelic acid or 2-(6-methoxy-2-naphthyl)propanoic acid in a suitable solvent such as THF, acetonitrile or isopropyl alcohol.
  • the chiral form (VIII) a may be liberated by treating the salt with a base, such as a resin-bound base, in a suitable solvent such as methanol.
  • Step (v) typically comprises treating a compound of formula (VIII) with a suitable amine protecting reagent, such as Boc 2 O, in the presence of a suitable solvent, such as dichloromethane (DCM).
  • a suitable amine protecting reagent such as Boc 2 O
  • Step (vi) typically comprises reacting a terminal alkyne of formula (IX) or (VIII) with a compound of formula (X) in the presence of a suitable reagent, such as copper iodide, a suitable catalyst, such as PdCl 2 (Ph 3 P) 2 , a suitable base, such as diethylamine (Et 2 NH) or diisopropylamine and a suitable solvent, such as tetrahydrofuran, or tertiarybutyl methyl ether.
  • a suitable reagent such as copper iodide
  • a suitable catalyst such as PdCl 2 (Ph 3 P) 2
  • a suitable base such as diethylamine (Et 2 NH) or diisopropylamine
  • a suitable solvent such as tetrahydrofuran, or tertiarybutyl methyl ether.
  • Step (vii) typically comprises deprotecting a compound of formula (XI) with a suitable acidic reagent, such as trifluoroacetic acid (TFA) in the presence of a suitable solvent, such as dichloromethane (DCM) or alternatively by using sulphuric acid in a solvent such as 1,4-dioxane.
  • a suitable acidic reagent such as trifluoroacetic acid (TFA)
  • TFA trifluoroacetic acid
  • DCM dichloromethane
  • sulphuric acid in a solvent such as 1,4-dioxane.
  • L 1 represents a suitable leaving group, such as a halogen atom (i.e. bromine) and L 2 represents a suitable leaving group, such as a halogen atom (i.e. iodine), P 2 represents a suitable protecting group, such as SEM and P 3 represents a suitable protecting group, such as Boc 2 O.
  • a suitable leaving group such as a halogen atom (i.e. bromine)
  • L 2 represents a suitable leaving group, such as a halogen atom (i.e. iodine)
  • P 2 represents a suitable protecting group, such as SEM
  • P 3 represents a suitable protecting group, such as Boc 2 O.
  • Step (i) typically comprises reacting a compound of formula (XII) with a compound of formula (IV) in the presence of a suitable solvent, such as dichloroethane (DCE).
  • a suitable solvent such as dichloroethane (DCE).
  • Step (ii) typically comprises introducing a protecting group by reacting a compound of formula (XIII) with, for example SEM-CI, in the presence of potassium tert-butoxide and a suitable solvent, such as tetrahydrofuran (THF).
  • a protecting group by reacting a compound of formula (XIII) with, for example SEM-CI, in the presence of potassium tert-butoxide and a suitable solvent, such as tetrahydrofuran (THF).
  • Step (iii) typically comprises reacting a compound of formula (XIV) with a compound of formula (VI) in the presence of potassium tert-butoxide and a suitable solvent, such as tetrahydrofuran (THF).
  • a suitable solvent such as tetrahydrofuran (THF).
  • Step (iv) typically comprises deprotecting a compound of formula (XV) with a suitable acidic reagent, such as citric acid.
  • Step (v) typically comprises treating a compound of formula (XVI) with a suitable protecting group, such as Boc 2 O, in the presence of a suitable solvent, such as dichloromethane (DCM).
  • a suitable protecting group such as Boc 2 O
  • DCM dichloromethane
  • Step (vi) typically comprises reacting a compound of formula (XVII) with a compound of formula (X) in the presence of a suitable reagent, such as copper iodide, a suitable catalyst, such as PdCl 2 (Ph 3 P) 2 , a suitable base, such as diethylamine (Et 2 NH) and a suitable solvent, such as tetrahydrofuran or tertiary butyl methyl ether.
  • a suitable reagent such as copper iodide
  • a suitable catalyst such as PdCl 2 (Ph 3 P) 2
  • a suitable base such as diethylamine (Et 2 NH)
  • a suitable solvent such as tetrahydrofuran or tertiary butyl methyl ether.
  • Step (vii) typically comprises deprotecting a compound of formula (XVIII) with a suitable acidic reagent, such as trifluoroacetic acid (TFA) in the presence of a suitable solvent, such as dichloromethane (DCM).
  • a suitable acidic reagent such as trifluoroacetic acid (TFA)
  • TFA trifluoroacetic acid
  • DCM dichloromethane
  • L 2 represents a suitable leaving group, such as a halogen atom (i.e. iodine)
  • L 3 represents a suitable leaving group, such as a halogen atom (i.e. chlorine)
  • L 4 represents a suitable leaving group, such as a halogen atom (i.e. chlorine).
  • Step (i) typically comprises reacting a compound of formula (XX) with a compound of formula (XXI) in the presence of a suitable reagent, such as sodium carbonate, a suitable catalyst, such as PdCl 2 (Ph 3 P) 2 , and a suitable solvent, such as dimethoxyethane/water.
  • a suitable reagent such as sodium carbonate
  • a suitable catalyst such as PdCl 2 (Ph 3 P) 2
  • a suitable solvent such as dimethoxyethane/water.
  • step (ii) typically comprises reacting a compound of formula (MI) with hydrogen iodide.
  • R 1 , R 2 , R 4 , R 9 , m, n, q, A and Y are as defined herein for compounds of formula (I).
  • Step (i) typically comprises condensation of a compound of formula (III) with a carboxyaldehyde compound, including for example a compound of formula (XXVII) (the preparation of which is described below in Scheme 5), in the presence of a dehydrating agent such as magnesium sulfate, or molecular sieves, in a solvent such as dichloromethane.
  • a dehydrating agent such as magnesium sulfate, or molecular sieves
  • Step (ii) typically comprises a [3+2] cycloaddition reaction with phenyl vinyl sulfone catalysed by a transition metal salt such as a silver or copper salt, in the presence of a base and optionally a chiral phosphine ligand.
  • a transition metal salt such as a silver or copper salt
  • Step (iii) typically comprises elimination of the phenyl vinyl sulfone typically with a strong base such as potassium tert-butoxide.
  • Carboxaldehyde compounds of formula (XXVII) suitable for reacting with compounds of formula (III) in Scheme 4 may be commercially available but may also be prepared according to Scheme 5:
  • Step (i) typically comprises an acid catalysed (for example hydrochloride acid) alkoholysis of a 2-cyanopyrimdine with, for example, methanol.
  • an acid catalysed (for example hydrochloride acid) alkoholysis of a 2-cyanopyrimdine with, for example, methanol for example, an acid catalysed (for example hydrochloride acid) alkoholysis of a 2-cyanopyrimdine with, for example, methanol.
  • Step (ii) comprises a reduction to an aldehyde using a hindered hydride reducing agent, for example diisobutyl aluminium hydride, in a suitable solvent such as toluene or dichloromethane.
  • a hindered hydride reducing agent for example diisobutyl aluminium hydride
  • Step (i) typically comprises a Horner-Wadsworth-Emmons condensation reaction of an optionally substituted carbamate protected alpha aminocarboxaldehyde with an optionally substituted methyl 2-(tert-butoxycarbonylamino)phosphorylacetate in the presence of a catalyst such as 1,8-diazabicyclo(5.4.0)undec-7-ene.
  • a catalyst such as 1,8-diazabicyclo(5.4.0)undec-7-ene.
  • Step (ii) typically comprises a hydrogenation such as continuous hydrogenation reaction performed in a flow system, for example by using a hydrogenation reactor such as an H-cube, and passing a flow of substrate through a packed catalyst cartridge.
  • a hydrogenation reactor such as an H-cube
  • Step (iii) typically comprises deprotection of the amine group with a strong acid such as HCl in a solvent such as dioxane.
  • the salt form of (III) may be converted to the free base form by treatment with a base such as triethylamine in the course of a subsequent reaction.
  • interconversion reaction typically comprises a suitable base such as sodium hydride to deprotonate the amide followed by treatment with an alkylating agent such as methyl iodide in a solvent such as DMF.
  • One further particular interconversion which may be mentioned includes alkylation of compounds of formula (I) wherein R 3 represents hydrogen to a compound of formula (I) wherein R 3 represents C 1-6 alkyl.
  • Such an interconversion reaction typically comprises reductive alkylation with an aldehyde in the presence of a suitable mild hydride donor agent such as sodium triacetoxyborohydride.
  • isomer separation may occur at any suitable stage in the synthetic sequence. It should be stressed that such chiral separation forms a key aspect of the invention and that such separation may be conducted in accordance with the methodology described herein or may be conducted in accordance with known methodology.
  • a compound of formula (VIII) including the case where R 4 ⁇ H, may be resolved into component enantiomers by resolution to form differentially soluble and separable diastereomeric crystalline salts with a chiral acid such as mandelic acid, 2-methoxy-2-phenylacetic acid, tartaric acid, camphor sulfonic acid or di-p-toluoyltartaric acid, followed by treatment with base to liberate the resolved free base form.
  • a hydroxy group may be protected, for example, as an ether (—OR) or an ester (—OC( ⁇ O)R), for example, as: a t-butyl ether; a tetrahydropyranyl (THP) ether; a benzyl, benzhydryl (diphenylmethyl), or trityl (triphenylmethyl) ether; a trimethylsilyl or t-butyldimethylsilyl ether; or an acetyl ester (—OC( ⁇ O)CH 3 ).
  • an ether —OR
  • an ester —OC( ⁇ O)R
  • the aldehyde or ketone group is readily regenerated by hydrolysis using a large excess of water in the presence of acid.
  • An amine group may be protected, for example, as an amide (—NRCO—R) or a carbamate (—NRCO—OR), for example, as: a methyl amide (—NHCO—CH 3 ); a benzyl carbamate (—NHCO—OCH 2 C 6 H 5 , —NH-Cbz or NH—Z); as a t-butyl carbamate (—NHCO—OC(CH 3 ) 3 , —NH-Boc); a 2-biphenyl-2-propyl carbamate (—NHCO—OC(CH 3 ) 2 C 6 H 4 C 6 H 5 , —NH-Boc), as a 9-fluorenylmethyl carbamate (—NH-Fmoc), as a 6-nitroveratryl carbamate (—NH—Nvoc), as a 2-trimethylsilylethyl carbamate (—NH-Teoc), as a 2,2,2-trichloroethyl carbamate (
  • protecting groups for amines include toluenesulphonyl (tosyl) and methanesulphonyl (mesyl) groups, benzyl groups such as a para-methoxybenzyl (PMB) group and tetrahydropyranyl (THP) groups.
  • tosyl toluenesulphonyl
  • methanesulphonyl methanesulphonyl
  • benzyl groups such as a para-methoxybenzyl (PMB) group and tetrahydropyranyl (THP) groups.
  • PMB para-methoxybenzyl
  • THP tetrahydropyranyl
  • compounds of the invention may be useful for the treatment of diseases and conditions mediated by modulation of voltage-gated sodium channels.
  • the compounds will be state-dependent sodium channel inhibitors.
  • the compounds will be subtype NaV1.7 sodium channel state-dependent inhibitors.
  • the compounds will be state-dependent sodium channel inhibitors which have a suitable developability profile on oral administration, for example in terms of exposure (Cmax) and/or bioavailability.
  • the compounds will be sodium channel inhibitors.
  • the compounds will be subtype NaV1.7 sodium channel inhibitors.
  • the compounds will be sodium channel inhibitors which have a suitable developability profile on oral administration, for example in terms of exposure (Cmax) and/or bioavailability.
  • compounds of the invention for use as a medicament, preferably a human medicament.
  • the invention provides the use of compounds of the invention in the manufacture of a medicament for treating or preventing a disease or condition mediated by modulation of voltage-gated sodium channels.
  • compounds of the invention may be useful as analgesics.
  • they may be useful in the treatment of chronic inflammatory pain (e.g. pain associated with rheumatoid arthritis, osteoarthritis, rheumatoid spondylitis, gouty arthritis and juvenile arthritis); musculoskeletal pain; lower back and neck pain; sprains and strains; neuropathic pain; sympathetically maintained pain; myositis; pain associated with cancer and fibromyalgia; pain associated with migraine; pain associated with influenza or other viral infections, such as the common cold; rheumatic fever; pain associated with functional bowel disorders such as non-ulcer dyspepsia, non-cardiac chest pain and irritable bowel syndrome; pain associated with myocardial ischemia; post operative pain; headache; toothache; and dysmenorrhea.
  • chronic inflammatory pain e.g. pain associated with rheumatoid arthritis, osteoarthritis, rheumatoid
  • Neuropathic pain syndromes can develop following neuronal injury and the resulting pain may persist for months or years, even after the original injury has healed.
  • Neuronal injury may occur in the peripheral nerves, dorsal roots, spinal cord or certain regions in the brain.
  • Neuropathic pain syndromes are traditionally classified according to the disease or event that precipitated them.
  • Neuropathic pain syndromes include: diabetic neuropathy; sciatica; non-specific lower back pain; multiple sclerosis pain; fibromyalgia; HIV-related neuropathy; post-herpetic neuralgia; trigeminal neuralgia; and pain resulting from physical trauma, amputation, cancer, toxins or chronic inflammatory conditions.
  • neuropathic pain are incredibly heterogeneous and are often described as spontaneous shooting and lancinating pain, or ongoing, burning pain.
  • pain associated with normally non-painful sensations such as “pins and needles” (paraesthesias and dysesthesias), increased sensitivity to touch (hyperesthesia), painful sensation following innocuous stimulation (dynamic, static or thermal allodynia), increased sensitivity to noxious stimuli (thermal, cold, mechanical hyperalgesia), continuing pain sensation after removal of the stimulation (hyperpathia) or an absence of or deficit in selective sensory pathways (hypoalgesia).
  • Compounds of the invention may also be useful in the amelioration of inflammatory disorders, for example in the treatment of skin conditions (e.g. sunburn, burns, eczema, dermatitis, psoriasis); ophthalmic diseases; lung disorders (e.g. asthma, bronchitis, emphysema, allergic rhinitis, non-allergic rhinitis, cough, respiratory distress syndrome, pigeon fancier's disease, farmer's lung, chronic obstructive pulmonary disease, (COPD); gastrointestinal tract disorders (e.g.
  • the compounds of the invention are useful in the treatment of neuropathic pain or inflammatory pain as described herein.
  • Alzheimer's disease includes primary sleep disorders such as Dyssomnias such as Primary Insomnia (307.42), Primary Hypersomnia (307.44), Narcolepsy (347), Breathing-Related Sleep Disorders (780.59), Circadian Rhythm Sleep Disorder (307.45) and Dyssomnia Not Otherwise Specified (307.47); primary sleep disorders such as Parasomnias such as Nightmare Disorder (307.47), Sleep Terror Disorder (307.46), Sleepwalking Disorder (307.46) and Parasomnia Not Otherwise Specified (307.47); Sleep Disorders Related to Another Mental Disorder such as Insomnia Related to Another Mental Disorder (307.42) and Hypersomnia Related to Another Mental Disorder (307.44); Sleep Disorder Due to a General Medical Condition, in particular sleep disturbances associated with such diseases as neurological disorders, neuropathic pain, restless leg syndrome, heart and lung diseases; and Substance-Induced Sleep Disorder including the subtypes Insomnia Type, Hypersomnia Type, Parasomnia Type and Mixed Type; sleep apn
  • Attention-Deficit/Hyperactivity Disorder including the subtypes Attention-Deficit/Hyperactivity Disorder Combined Type (314.01), Attention-Deficit/Hyperactivity Disorder Predominantly Inattentive Type (314.00), Attention-Deficit/Hyperactivity Disorder Hyperactive-Impulse Type (314.01) and Attention-Deficit/Hyperactivity Disorder Not Otherwise Specified (314.9); Hyperkinetic Disorder; Disruptive Behaviour Disorders such as Conduct Disorder including the subtypes childhood-onset type (321.81), Adolescent-Onset Type (312.82) and Unspecified Onset (312.89), Oppositional Defiant Disorder (313.81) and Disruptive Behaviour Disorder Not Otherwise Specified; and Tic Disorders such as Tourette's Disorder (307.23): ix) Personality Disorders including the subtypes Paranoid Personality Disorder (301.0), Schizoid Personality Disorder (301.20), Schizotypal Personality Disorder (301,22), Antisocial Personality Disorder
  • Impulse control disorder including: Intermittent Explosive Disorder (312.34), Kleptomania (312.32), Pathological Gambling (312.31), Pyromania (312.33), Trichotillomania (312.39), Impulse-Control Disorders Not Otherwise Specified (312.3), Binge Eating, Compulsive Buying, Compulsive Sexual Behaviour and Compulsive Hoarding.
  • diseases or conditions that may be mediated by modulation of voltage gated sodium channels are depression or mood disorders
  • diseases or conditions that may be mediated by modulation of voltage gated sodium channels are substance related disorders.
  • diseases or conditions that may be mediated by modulation of voltage gated sodium channels are Bipolar Disorders (including Bipolar I Disorder, Bipolar II Disorder (i.e. Recurrent Major Depressive Episodes with Hypomanic Episodes) (296.89), Cyclothymic Disorder (301.13) or Bipolar Disorder Not Otherwise Specified (296.80)).
  • Bipolar Disorders including Bipolar I Disorder, Bipolar II Disorder (i.e. Recurrent Major Depressive Episodes with Hypomanic Episodes) (296.89), Cyclothymic Disorder (301.13) or Bipolar Disorder Not Otherwise Specified (296.80)
  • diseases or conditions that may be mediated by modulation of voltage gated sodium channels are Nicotine-Related Disorders such as Nicotine Dependence (305.1), Nicotine Withdrawal (292.0) or Nicotine-Related Disorder Not Otherwise Specified (292.9).
  • Compounds of the invention may also be useful in the treatment and/or prevention of disorders treatable and/or preventable with anti-convulsive agents, such as epilepsy including post-traumatic epilepsy, obsessive compulsive disorders (OCD), sleep disorders (including circadian rhythm disorders, insomnia & narcolepsy), tics (e.g. Giles de la Tourette's syndrome), ataxias, muscular rigidity (spasticity), and temporomandibular joint dysfunction.
  • epilepsy including post-traumatic epilepsy, obsessive compulsive disorders (OCD), sleep disorders (including circadian rhythm disorders, insomnia & narcolepsy), tics (e.g. Giles de la Tourette's syndrome), ataxias, muscular rigidity (spasticity), and temporomandibular joint dysfunction.
  • OCD obsessive compulsive disorders
  • sleep disorders including circadian rhythm disorders, insomnia & narcolepsy
  • tics e.g. Gi
  • Compounds of the invention may also be useful in the treatment of bladder hyperrelexia following bladder inflammation.
  • Compounds of the invention may also be useful in the treatment of neurodegenerative diseases and neurodegeneration such as dementia, particularly degenerative dementia (including senile dementia, Alzheimer's disease, Pick's disease, Huntington's chorea, Parkinson's disease and Creutzfeldt-Jakob disease, motor neuron disease);
  • the compounds may also be useful for the treatment of amyotrophic lateral sclerosis (ALS) and neuroinflamation.
  • ALS amyotrophic lateral sclerosis
  • Compounds of the invention may also be useful in neuroprotection and in the treatment of neurodegeneration following stroke, cardiac arrest, pulmonary bypass, traumatic brain injury, spinal cord injury or the like.
  • Compounds of the invention may also be useful in the treatment of tinnitus, and as local anaesthetics.
  • the compounds of the invention may also be used in combination with other therapeutic agents.
  • the invention thus provides, in a further aspect, a combination comprising a compound of the invention or a pharmaceutically acceptable derivative thereof together with a further therapeutic agent.
  • a compound of the invention or a pharmaceutically acceptable derivative thereof When a compound of the invention or a pharmaceutically acceptable derivative thereof is used in combination with a second therapeutic agent active against the same disease state the dose of each compound may differ from that when the compound is used alone. Appropriate doses will be readily appreciated by those skilled in the art. It will be appreciated that the amount of a compound of the invention required for use in treatment will vary with the nature of the condition being treated and the age and the condition of the patient and will be ultimately at the discretion of the attendant physician or veterinarian.
  • compositions comprising a combination as defined above together with a pharmaceutically acceptable carrier or excipient comprise a further aspect of the invention.
  • the individual components of such combinations may be administered either sequentially or simultaneously in separate or combined pharmaceutical formulations by any convenient route.
  • either the compound of the invention or the second therapeutic agent may be administered first.
  • the combination may be administered either in the same or different pharmaceutical composition.
  • the two compounds When combined in the same formulation it will be appreciated that the two compounds must be stable and compatible with each other and the other components of the formulation. When formulated separately they may be provided in any convenient formulation, conveniently in such manner as are known for such compounds in the art.
  • the compound of formula (I) or a pharmaceutically acceptable salt thereof may be used in combination with other medicaments indicated to be useful in the treatment or prophylaxis of pain of neuropathic origin including neuralgias, neuritis and back pain, and inflammatory pain including osteoarthritis, rheumatoid arthritis, acute inflammatory pain, back pain and migraine.
  • Such therapeutic agents include for example COX-2 (cyclooxygenase-2) inhibitors, such as celecoxib, deracoxib, rofecoxib, valdecoxib, parecoxib, COX-189 or 2-(4-ethoxy-phenyl)-3-(4-methanesulfonyl-phenyl)-pyrazolo[1,5-b]pyridazine (WO 99/012930); 5-lipoxygenase inhibitors; NSAIDs (non-steroidal anti-inflammatory drugs) such as diclofenac, indomethacin, nabumetone or ibuprofen; bisphosphonates, leukotriene receptor antagonists; DMARDs (disease modifying anti-rheumatic drugs) such as methotrexate; adenosine A1 receptor agonists; sodium channel blockers, such as lamotrigine; NMDA (N-methyl-D-aspartate) receptor modulators, such
  • the compounds of the invention may be used in combination with the following agents to treat or prevent psychotic disorders: i) antipsychotics; ii) drugs for extrapyramidal side effects, for example anticholinergics (such as benztropine, biperiden, procyclidine and trihexyphenidyl), antihistamines (such as diphenhydramine) and dopaminergics (such as amantadine); iii) antidepressants; iv) anxiolytics; and v) cognitive enhancers for example cholinesterase inhibitors (such as tacrine, donepezil, rivastigmine and galantamine).
  • anticholinergics such as benztropine, biperiden, procyclidine and trihexyphenidyl
  • antihistamines such as diphenhydramine
  • dopaminergics such as amantadine
  • antidepressants such as amantadine
  • iv) anxiolytics such as anxio
  • the compounds of the invention may be used in combination with the following agents to treat or prevent psychotic disorders: i) antipsychotics; ii) drugs for extrapyramidal side effects, for example anticholinergics (such as benztropine, biperiden, procyclidine and trihexyphenidyl), antihistamines (such as diphenhydramine) and dopaminergics (such as amantadine); iii) antidepressants; iv) anxiolytics; and v) cognitive enhancers for example cholinesterase inhibitors (such as tacrine, donepezil, rivastigmine and galantamine).
  • anticholinergics such as benztropine, biperiden, procyclidine and trihexyphenidyl
  • antihistamines such as diphenhydramine
  • dopaminergics such as amantadine
  • antidepressants such as amantadine
  • iv) anxiolytics such as anxio
  • the compounds of the invention may be used in combination with antidepressants to treat or prevent depression and mood disorders.
  • the compounds of the invention may be used in combination with the following agents to treat or prevent bipolar disease: i) mood stabilisers; ii) antipsychotics; and iii) antidepressants.
  • the compounds of the invention may be used in combination with the following agents to treat or prevent anxiety disorders: i) anxiolytics; and ii) antidepressants.
  • the compounds of the invention may be used in combination with the following agents to improve nicotine withdrawal and reduce nicotine craving: i) nicotine replacement therapy for example a sublingual formulation of nicotine beta-cyclodextrin and nicotine patches; and ii) bupropion.
  • the compounds of the invention may be used in combination with the following agents to improve alcohol withdrawal and reduce alcohol craving: i) NMDA receptor antagonists for example acamprosate; ii) GABA receptor agonists for example tetrabamate; and iii) Opioid receptor antagonists for example naltrexone.
  • NMDA receptor antagonists for example acamprosate
  • GABA receptor agonists for example tetrabamate
  • Opioid receptor antagonists for example naltrexone.
  • the compounds of the invention may be used in combination with the following agents to improve opiate withdrawal and reduce opiate craving: i) opioid mu receptor agonist/opioid kappa receptor antagonist for example buprenorphine; ii) opioid receptor antagonists for example naltrexone; and iii) vasodilatory antihypertensives for example Iofexidine.
  • opioid mu receptor agonist/opioid kappa receptor antagonist for example buprenorphine
  • opioid receptor antagonists for example naltrexone
  • vasodilatory antihypertensives for example Iofexidine.
  • the compounds of the invention may be used in combination with the following agents to treat or prevent sleeping disorders: i) benzodiazepines for example temazepam, lormetazepam, estazolam and triazolam; ii) non-benzodiazepine hypnotics for example zolpidem, zopiclone, zaleplon and indiplon; iii) barbiturates for example aprobarbital, butabarbital, pentobarbital, secobarbita and phenobarbital; iv) antidepressants; v) other sedative-hypnotics for example chloral hydrate and chlormethiazole.
  • benzodiazepines for example temazepam, lormetazepam, estazolam and triazolam
  • non-benzodiazepine hypnotics for example zolpidem, zopiclone, zaleplon and indiplon
  • barbiturates for example
  • the compounds of the invention may be used in combination with the following agents to treat anorexia: i) appetite stimulants for example cyproheptidine; ii) antidepressants; iii) antipsychotics; iv) zinc; and v) premenstrual agents for example pyridoxine and progesterones.
  • the compounds of the invention may be used in combination with the following agents to treat or prevent bulimia: i) antidepressants; ii) opioid receptor antagonists; iii) antiemetics for example ondansetron; iv) testosterone receptor antagonists for example flutamide; v) mood stabilisers; vi) zinc; and vii) premenstrual agents.
  • the compounds of the invention may be used in combination with the following agents to treat or prevent autism: i) antipsychotics; ii) antidepressants; iii) anxiolytics; and iv) stimulants for example methylphenidate, amphetamine formulations and pemoline.
  • the compounds of the invention may be used in combination with the following agents to treat or prevent ADHD: i) stimulants for example methylphenidate, amphetamine formulations and pemoline; and ii) non-stimulants for example norepinephrine reuptake inhibitors (such as atomoxetine), alpha 2 adrenoceptor agonists (such as clonidine), antidepressants, modafinil, and cholinesterase inhibitors (such as galantamine and donezepil).
  • stimulants for example methylphenidate, amphetamine formulations and pemoline
  • non-stimulants for example norepinephrine reuptake inhibitors (such as atomoxetine), alpha 2 adrenoceptor agonists (such as clonidine), antidepressants, modafinil, and cholinesterase inhibitors (such as galantamine and donezepil).
  • the compounds of the invention may be used in combination with the following agents to treat personality disorders: i) antipsychotics; ii) antidepressants; iii) mood stabilisers; and iv) anxiolytics.
  • the compounds of the invention may be used in combination with the following agents to treat or prevent male sexual dysfunction: i) phosphodiesterase V inhibitors, for example vardenafil and sildenafil; ii) dopamine agonists/dopamine transport inhibitors for example apomorphine and bupropion; iii) alpha adrenoceptor antagonists for example phentolamine; iv) prostaglandin agonists for example alprostadil; v) testosterone agonists such as testosterone; vi) serotonin transport inhibitors for example serotonin reuptake inhibitors; v) noradrenaline transport inhibitors for example reboxetine and vii) 5-HT1A agonists, for example flibanserine.
  • phosphodiesterase V inhibitors for example vardenafil and sildenafil
  • dopamine agonists/dopamine transport inhibitors for example apomorphine and bupropion
  • alpha adrenoceptor antagonists
  • the compounds of the invention may be used in combination with the same agents specified for male sexual dysfunction to treat or prevent female sexual dysfunction, and in addition an estrogen agonist such as estradiol.
  • Antipsychotic drugs include Typical Antipsychotics (for example chlorpromazine, thioridazine, mesoridazine, fluphenazine, perphenazine, proclorperazine, trifluoperazine, thiothixene, haloperidol, molindone and loxapine); and Atypical Antipsychotics (for example clozapine, olanzapine, risperidone, quetiapine, aripiprazole, ziprasidone and amisulpride).
  • Antidepressant drugs include serotonin reuptake inhibitors (such as citalopram, escitalopram, fluoxetine, paroxetine and sertraline); dual serotonin/noradrenaline reuptake inhibitors (such as venlafaxine, duloxetine and milnacipran); Noradrenaline reuptake inhibitors (such as reboxetine); tricyclic antidepressants (such as amitriptyline, clomipramine, imipramine, maprotiline, nortriptyline and trimipramine); monoamine oxidase inhibitors (such as isocarboxazide, moclobemide, phenelzine and tranylcypromine); and others (such as bupropion, mianserin, mirtazapine, nefazodone and trazodone).
  • serotonin reuptake inhibitors such as citalopram, escitalopram, fluoxetine, parox
  • Mood stabiliser drugs include lithium, sodium valproate/valproic acid/divalproex, carbamazepine, lamotrigine, gabapentin, topiramate and tiagabine.
  • Anxiolytics include benzodiazepines such as alprazolam and lorazepam.
  • references herein to “treatment” extend to prophylaxis, prevention of recurrence and suppression or amelioration of symptoms (whether mild, moderate or severe) as well as the treatment of established conditions.
  • the compound of the invention may be administered as the raw chemical but the active ingredient is preferably presented as a pharmaceutical formulation.
  • the invention provides a pharmaceutical composition
  • a pharmaceutical composition comprising a compound of the invention, in association with one or more pharmaceutically acceptable carrier(s), diluents(s) and/or excipient(s).
  • the carrier, diluent and/or excipient must be “acceptable” in the sense of being compatible with the other ingredients of the composition and not deleterious to the recipient thereof.
  • the compounds of the invention may be administered in conventional dosage forms prepared by combining a compound of the invention with standard pharmaceutical carriers or diluents according to conventional procedures well known in the art. These procedures may involve mixing, granulating and compressing or dissolving the ingredients as appropriate to the desired preparation.
  • compositions of the invention may be formulated for administration by any route, and include those in a form adapted for oral, topical or parenteral administration to mammals including humans.
  • compositions may be in the form of tablets, capsules, powders, granules, lozenges, creams or liquid preparations, such as oral or sterile parenteral solutions or suspensions.
  • topical formulations of the present invention may be presented as, for instance, ointments, creams or lotions, eye ointments and eye or ear drops, impregnated dressings and aerosols, and may contain appropriate conventional additives such as preservatives, solvents to assist drug penetration and emollients in ointments and creams.
  • the formulations may also contain compatible conventional carriers, such as cream or ointment bases and ethanol or oleyl alcohol for lotions.
  • suitable conventional carriers such as cream or ointment bases and ethanol or oleyl alcohol for lotions.
  • Such carriers may be present as from about 1% up to about 98% of the formulation. More usually they will form up to about 80% of the formulation.
  • Tablets and capsules for oral administration may be in unit dose presentation form, and may contain conventional excipients such as binding agents, for example syrup, acacia, gelatine, sorbitol, tragacanth, or polyvinylpyrrolidone; fillers, for example lactose, sugar, maize-starch, calcium phosphate, sorbitol or glycine; tabletting lubricants, for example magnesium stearate, talc, polyethylene glycol or silica; disintegrants, for example potato starch; or acceptable wetting agents such as sodium lauryl sulphate.
  • the tablets may be coated according to methods well known in normal pharmaceutical practice.
  • Oral liquid preparations may be in the form of, for example, aqueous or oily suspensions, solutions, emulsions, syrups or elixirs, or may be presented as a dry product for reconstitution with water or other suitable vehicle before use.
  • Such liquid preparations may contain conventional additives, such as suspending agents, for example sorbitol, methyl cellulose, glucose syrup, gelatine, hydroxyethyl cellulose, carboxymethyl cellulose, aluminium stearate gel or hydrogenated edible fats, emulsifying agents, for example lecithin, sorbitan monooleate, or acacia; non-aqueous vehicles (which may include edible oils), for example almond oil, oily esters such as glycerine, propylene glycol, or ethyl alcohol; preservatives, for example methyl or propyl p-hydroxybenzoate or sorbic acid, and, if desired, conventional flavouring or colouring agents.
  • suspending agents for example sorbitol, methyl cellulose, glucose syrup, gelatine, hydroxyethyl cellulose, carboxymethyl cellulose, aluminium stearate gel or hydrogenated edible fats, emulsifying agents, for example lecithin, sorbitan monooleate
  • Suppositories will contain conventional suppository bases, e.g. cocoa-butter or other glyceride.
  • fluid unit dosage forms are prepared utilising the compound and a sterile vehicle, water being preferred.
  • the compound depending on the vehicle and concentration used, can be either suspended or dissolved in the vehicle.
  • the compound can be dissolved in water for injection and filter-sterilised before filling into a suitable vial or ampoule and sealing.
  • agents such as a local anaesthetic, preservative and buffering agents can be dissolved in the vehicle.
  • the composition can be frozen after filling into the vial and the water removed under vacuum.
  • the dry lyophilised powder is then sealed in the vial and an accompanying vial of water for injection may be supplied to reconstitute the liquid prior to use.
  • Parenteral suspensions are prepared in substantially the same manner except that the compound is suspended in the vehicle instead of being dissolved and sterilisation cannot be accomplished by filtration.
  • the compound can be sterilised by exposure to ethylene oxide before suspending in the sterile vehicle.
  • a surfactant or wetting agent is included in the composition to facilitate uniform distribution of the compound.
  • compositions may contain from 0.1% by weight, for example from 10-60% by weight, of the active material, depending on the method of administration. Where the compositions comprise dosage units, each unit will for example contain from 5-1000 mg of the active ingredient.
  • the dosage as employed for adult human treatment may range from 10 to 3000 mg per day depending on the route and frequency of administration. For oral administration a typical dose may be in the range of 50 to 1500 mg per day, for example 120 to 1000 mg per day.
  • the optimal quantity and spacing of individual dosages of a compound of the invention will be determined by the nature and extent of the condition being treated, the form, route and site of administration, and the particular mammal being treated, and that such optimums can be determined by conventional techniques. It will also be appreciated by one of skill in the art that the optimal course of treatment, i.e., the number of doses of a compound of the invention given per day for a defined number of days, can be ascertained by those skilled in the art using conventional course of treatment determination tests.
  • NMR spectra are typically recorded on a Bruker instruments at 300, 400 or 500 MHz. Chemical shifts are reported in ppm ( ⁇ ) using the residual solvent line as internal standard. Splitting patterns are designated as s, singlet; d, doublet; t, triplet; q, quartet; m, multiplet; br, broad. The NMR spectra were recorded at a temperature ranging from 25 to 90° C. When more than one conformer was detected the chemical shifts for the most abundant one is reported.
  • LC-MS Data is typically generated on an Waters ZQ Mass Spectrometer, operating in switched ES+ and ES ⁇ ionization modes coupled to an Agilent 1100 Series HPLC system with in line Aglient 1100 UV-DAD and Sedere SEDEX 75 ELSD Detection. Instrument control and data acquisition is mediated through the Waters MassLynx-OpenLynx software suite. Separation was performed on a Waters SunFire C18 (30 ⁇ 4.6 mm, 3.5 ⁇ m) column Flow Rate: 3.0 mL/min. column temperature 30° C. Injection Volume: 5.0 ⁇ L.
  • Chiral chromatography was typically performed using a ChiralPakTM AD-H or IA column from Daicel® using heptane/ethanol or heptane/ethanol/methanol mixtures as eluent.
  • Analytical chiral HPLC was carried out either on an Agilent 1100 series HPLC system or on a Gilson HPLC system using a 250 ⁇ 4.6 mm column and a flow rate of 1 ml/min.
  • Preparative chiral HPLC was carried out using a Gilson preparative HPLC system on a 250 ⁇ 19 mm semipreparative column with a flow rate of 18 ml/min.
  • Optical rotations were measured using an Optical Activity Ltd AA-10 automatic polarimeter (Cambridge, UK) using a cell of 10 cm path length and in chloroform solution unless otherwise indicated.
  • SCX cartridges are ion exchange solid phase extraction columns supplied by Varian.
  • the eluent used with SCX cartridges is methanol followed by 0.2-2.0 M ammonia solution in methanol.
  • Benzophenone imine [CAS: 1013-88-3] (16.67 g, 91.98 mmol) was added dropwise to a solution of 3-amino-1-methylpyrrolidine-2-one [CAS 119329-48-5] (10 g, 87.60 mmol) in DCE (100 mL) under N 2 and the reaction was heated at reflux for 18 hours. The solvent was evaporated to afford an amber oil. This was purified using flash silica in a large sinter funnel, eluting with 4:1 to 3:7 i-hexane:EtOAc. An incomplete separation was achieved. 3-(Benzhydrylidene-amino)-1-methyl-pyrrolidin-2-one (D1) was isolated (25 g) with approximately 11% of an impurity present, but was used in the next step without further purification;
  • Benzophenone imine (200.04 g, 1103.8 mmol) was added dropwise over 20 minutes to a stirred solution of 3-amino-1-methylpyrrolidine-2-one (120 g, 1051.2 mmol) in DCE (1000 mL) at ambient temp under nitrogen in a 2 L flask fitted with a magnetic stirrer bar. The reagent was washed with further DCE (100 mL). The stirred solution was heated at reflux on a heat-on block at a block temp of 95° C. for 7 h, using a N 2 bubbler with exhaled gas passing through a safety trap then into 2 L of water via an upturned funnel (for scrubbing NH 3 gas, estimated to be approx 23 L).
  • Citric acid monohydrate (10.39 g, 49.46 mmol) was added to a solution of 3-(benzhydrylidene-amino)-1-methyl-3-prop-2-ynyl-pyrrolidin-2-one (6.26 g, 19.79 mmol) (which may be prepared as described in Description 2) in THF (150 mL) and the reaction was stirred at room temperature for 18 hours. A colourless solid precipitated out. The solvent was evaporated to give a gummy white solid. This was triturated with Et 2 O and the solid was washed with further Et 2 O.
  • Boc 2 O (944.75 mg, 4.33 mmol) was added to a solution of (3S)-3-amino-1-methyl-3-prop-2-ynyl-pyrrolidin-2-one (which may be prepared as described in Description 3) (549 mg, 3.61 mmol) in DCM (20 mL) at 20° C. and the reaction was stirred for 18 hrs.
  • Boc 2 O (2.77 g, 12.69 mmol) was added to a solution of (3S)-3-amino-1-methyl-3-prop-2-ynyl-pyrrolidin-2-one (which may be prepared as described in Description 3) (1.61 g, 10.58 mmol) in DCM (40 mL) at 20° C. and the reaction was stirred for 18 h. The reaction was warmed to 40° C. and stirred for a further 3 days.
  • Trifluoroacetic acid (2 mL, 26.9 mmol) was added to a solution of tert-butyl N-[(3S)-1-methyl-2-oxo-3-[3-[4-[4-(trifluoromethyl)phenyl]pyrimidin-2-yl]prop-2-ynyl]pyrrolidin-3-yl]carbamate (which may be prepared as described in Description 7) (555 mg, 1.17 mmol) in dichloromethane (10 mL) at 20° C. and the reaction was stirred for 1 hr. The reaction was quenched by the addition of sat. NaHCO 3 and the phases were separated.
  • Boc 2 O (777.8 mg, 3.56 mmol) was added to a solution of (3R)-3-amino-1-methyl-3-prop-2-ynyl-pyrrolidin-2-one (which may be prepared as described in Description 3) (452 mg, 2.97 mmol) in DCM (20 mL) at 20° C. and the reaction was stirred for 18 hrs.
  • tert-butyl N-[(3S)-1-methyl-2-oxo-3-prop-2-ynyl-pyrrolidin-3-yl]carbamate (which may be prepared as described in Description 4) (104.79 g, 415.32 mmol) was suspended in tert-Butyl methyl ether (2100 mL).
  • Trifluoroacetic acid (2 mL, 26.92 mmol) was added to a solution of tert-butyl N-[(3R)-1-methyl-3-[3-[4-methyl-6-[4-(trifluoromethyl)phenyl]pyrimidin-2-yl]prop-2-ynyl]-2-oxo-pyrrolidin-3-yl]carbamate (which may be prepared as described in Description 13) (482 mg, 0.99 mmol) in DCM (10 mL) at 20° C. and the reaction was stirred for 1 hour. Solid K 2 CO 3 was added to quench the TFA present (care: gas evolved) and the resultant solid was filtered off and washed five times with DCM.
  • Trifluoroacetic acid (5 mL, 67.31 mmol) was added to a solution of tert-butyl N-[(3S)-1-methyl-3-[3-[4-methyl-6-[4-(trifluoromethyl)phenyl]pyrimidin-2-yl]prop-2-ynyl]-2-oxo-pyrrolidin-3-yl]carbamate (3.83 g, 7.84 mmol) (which may be prepared as described in Description 13a) in DCM (50 mL) at 20° C. and the reaction was stirred overnight. The reaction was concentrated and a further portion of trifluoroacetic acid (2 ml) added.
  • reaction mixture was stirred at room temperature over 30 minutes.
  • the reaction was poured into a beaker and washed in with ethyl acetate (400 mL) and a little water.
  • the mixture was cooled to 15° C. and a solution of sodium carbonate (160 g in 1200 mL water) was added over 5 minutes.
  • the mixture was filtered over a pad of celite and the remaining solids washed with ethyl acetate (400 mL).
  • the filtrate phases were separated and the aqueous phase was extracted with ethyl acetate (2 ⁇ 400 mL).
  • the phases were separated and the organic layer treated with a solution of cysteine (100 g, 825.35 mmol) in water (1500 ml). This mixture was stirred vigorously for 30 minutes. The mixture was filtered through a pad of celite, and the celite washed with DCM (2 ⁇ 100 ml). The phases were separated and the organic layer placed in a large beaker. To this was added a solution of cysteine (50 g, 412.68 mmol) in water (500 ml) and the mixture was stirred for a further 30 minutes. The phases were separated and the organic layer was washed with a mixture of sat. brine (500 ml) and water (500 ml).
  • Trifluoroacetic acid (3 mL, 40.39 mmol) was added to a solution of tert-butyl N-[(3R)-3-[3-[4-(5-ethoxy-2-fluoro-phenyl)-6-methyl-pyrimidin-2-yl]prop-2-ynyl]-1-methyl-2-oxo-pyrrolidin-3-yl]carbamate (which may be prepared as described in Description 18) (605 mg, 1.25 mmol) in DCM (15 mL) at 20° C. and the reaction was stirred for 1 hour. Solid K 2 CO 3 was added to quench the TFA present (care: gas evolved) and the resultant solid was filtered off and washed five times with DCM.
  • Citric acid monohydrate (1.58 g, 7.5 mmol) was added to a solution of 3-(benzhydrylideneamino)-3-prop-2-ynyl-1-(2-trimethylsilylethoxymethyl)piperidin-2-one (which may be prepared as described in Description 23) (1.34 g, 3 mmol) in THF (30 mL) at 20° C. and the reaction was stirred for 5 days. The solution was evaporated and loaded onto an SCX cartridge (10 g) then eluted with MeOH, followed by 2M NH 3 in MeOH.
  • Boc 2 O (221.61 mg, 1.02 mmol) was added to a solution of (3S)-3-amino-3-prop-2-ynyl-1-(2-trimethylsilylethoxymethyl)piperidin-2-one (which may be prepared as described in Description 24) (239 mg, 0.85 mmol) in DCM (10 mL) at 20° C. and the reaction was stirred for 18 hrs. Washed with water, sat.
  • Trifluoroacetic acid (2 mL, 26.92 mmol) was added to a solution of the tert-butyl N-[(3S)-3-[3-[4-(5-ethoxy-2-fluoro-phenyl)-6-methyl-pyrimidin-2-yl]prop-2-ynyl]-2-oxo-1-(2-trimethylsilylethoxymethyl)-3-piperidyl]carbamate (which may be prepared as described in Description 26) (345 mg, 0.56 mmol) in DCM (10 mL) at 20° C. and the reaction was stirred for 18 hrs. The reaction was quenched by the addition of solid K 2 CO 3 and stirred for 5 mins.
  • EtOAc 250 ml was added and the mixture stirred vigorously for 0.5 h then filtered under suction through celite. The filtrate was transferred to a separating funnel and the layers separated. The aqueous fraction was further extracted with EtOAc (200 ml) and the combined organic extracts were dried (MgSO 4 ) and evaporated to a pale yellow, sticky solid. This was stirred with iso-hexane (30 ml) for 5 minutes then sonicated for 5 minutes.
  • the anti isomer B tert-butyl (2R,5S)-7-methyl-2-[4-methyl-6-[4-(trifluoromethyl)-phenyl]pyrimidin-2-yl]-6-oxo-1,7-diazaspiro[4.4]nonane-1-carboxylate (1.9 g, 3.8734 mmol, 70.3% yield), was obtained as a foam;
  • the dropping funnel was charged with a pre-sonicated solution of borane tert-butylamine (19.3 g, 221.87 mmol) in DCM (200 mL).
  • the borane complex was added slowly maintaining the temperature below ⁇ 70° C. over approx. 30 minutes. After addition the reaction was stirred at below ⁇ 70° C. for 90 minutes.
  • the dropping funnel was charged with 6M HCl (400 ml) and this was added dropwise over approx. 15 minutes. The reaction temperature warmed to ⁇ 50° C. during the addition. After addition was complete the acetone/dry-ice bath was removed and the reaction mixture warmed to room temperature then stirred for a further 30 minutes.
  • reaction mixture was cooled to ambient temperature and evaporated to an oil, which was applied to a 10 g cartridge and eluted on a Biotage SP4 system with a gradient of methanol in ethyl acetate. Relevant fractions were combined and evaporated to a solid, a racemic mixture of tert-butyl (2S,5S)- and (2R,5R)-2-[4-methyl-6-[4-(trifluoromethyl)phenyl]pyrimidin-2-yl]-6-oxo-1,7-diazaspiro[4.4]nonane-1-carboxylate (116 mg).
  • the compounds of the invention were tested in a QPatch NaV1.7 assay.
  • HEK293-hNaV1.7 cells were grown in DMEM-F12+10% FBS culture media at 37° C. At a confluency of 50-70% cells were dissociated from culture flasks & triturated to ensure unicellular cell suspension; cell density was measured & adjusted to 2-3 ⁇ 10 6 cells/ml. Recordings were obtained using QPatch16x.
  • the external solution was (in mM): NaCl, 128; KCl, 5; MgCl 2 , 2; CaCl 2 , 2; Glucose, 30; HEPES, 15; pH 7.3, 305-315 mOsm.
  • V1/2 SSI steady state inactivation voltage protocol
  • Two holding voltages were used to determine test drug inhibition: ⁇ 90 mV, where most of the channels are in a closed state; and V1/2 SSI, where half of the channels are inactivated.
  • Currents were elicited every 10 seconds by stepping to a membrane potential of 0 mV for 20 ms.
  • Four-point cumulative concentration responses were derived by determining the peak current amplitude at each concentration of test drug over 120 second application. Curves were fitted with the Hill equation yielding pIC50 values at ⁇ 90 mV and V1/2 SSI holding potentials.

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